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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Marchini J" with an ORCID

Julio Sergio Marchini
São Paulo University, Ribeirao Preto School of Medicine
117
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1,121
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Julio Marchini
No affiliation detected
17
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Joint testing of rare variant burden scores using non-negative least squares.
Ziyatdinov A, Mbatchou J, Marcketta A, Backman J, Gaynor S, Zou Y, Joseph T, Geraghty B, Herman J, Watanabe K, Ghosh A, Kosmicki J, Locke A, Regeneron Genetics Center, Thornton T, Kang HM, Ferreira M, Baras A, Abecasis G, Marchini J
Am J Hum Genet, 111(10):2139-2149, 01 Oct 2024
Cited by: 1 article | PMID: 39366334 | PMCID: PMC11480795
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Benfotiamine Supplementation Increases Thiamine in Muscle of Endurance-Trained Mice and Affects the Energy Metabolism.
Gonçalves ÁC, Vieira JF, Rodrigues ACN, Murta EFC, Marchini JS, Michelin MA, Portari GV
J Nutr Metab, 2024:6102611, 26 Sep 2024
Cited by: 0 articles | PMID: 39364430 | PMCID: PMC11449553
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Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank.
Gaynor SM, Joseph T, Bai X, Zou Y, Boutkov B, Maxwell EK, Delaneau O, Hofmeister RJ, Krasheninina O, Balasubramanian S, Marcketta A, Backman J, Regeneron Genetics Center, Reid JG, Overton JD, Lotta LA, Marchini J, Salerno WJ, Baras A, [...] Thornton TA
Nat Genet, 56(11):2345-2351, 25 Sep 2024
Cited by: 1 article | PMID: 39322778 | PMCID: PMC11549045
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Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone.
Dunn ME, Kithcart A, Kim JH, Ho AJ, Franklin MC, Romero Hernandez A, de Hoon J, Botermans W, Meyer J, Jin X, Zhang D, Torello J, Jasewicz D, Kamat V, Garnova E, Liu N, Rosconi M, Pan H, Karnik S, [...] Morton L
Nature, 633(8030):654-661, 11 Sep 2024
Cited by: 1 article | PMID: 39261724 | PMCID: PMC11410649
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NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.
Rodriguez-Flores JL, Khalid S, Parikshak N, Rasheed A, Ye B, Kapoor M, Backman J, Sepehrband F, Gioia SAD, Gelfman S, De T, Banerjee N, Sharma D, Martinez H, Castaneda S, D'Ambrosio D, Zhang XA, Xun P, Tsai E, [...] Saleheen D
Nat Commun, 15(1):8029, 13 Sep 2024
Cited by: 1 article | PMID: 39271666 | PMCID: PMC11399414
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Genetic risk factors for COVID-19 and influenza are largely distinct.
Kosmicki JA, Marcketta A, Sharma D, Di Gioia SA, Batista S, Yang XM, Tzoneva G, Martinez H, Sidore C, Kessler MD, Horowitz JE, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Leader JB, Park DS, Lanche R, Maxwell E, [...] Ferreira MAR
Nat Genet, 56(8):1592-1596, 05 Aug 2024
Cited by: 0 articles | PMID: 39103650 | PMCID: PMC11319199
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A Genomics England haplotype reference panel and imputation of UK Biobank.
Shi S, Rubinacci S, Hu S, Moutsianas L, Stuckey A, Need AC, Palamara PF, Caulfield M, Marchini J, Myers S
Nat Genet, 56(9):1800-1803, 12 Aug 2024
Cited by: 1 article | PMID: 39134668 | PMCID: PMC11387190
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Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk.
Vad OB, Monfort LM, Paludan-Müller C, Kahnert K, Diederichsen SZ, Andreasen L, Lotta LA, Nielsen JB, Lundby A, Svendsen JH, Olesen MS, Geisinger MyCode Community Health Initiative and the Regeneron Genetics Center (RGC) Research Team
JAMA Cardiol, 9(8):732-740, 01 Aug 2024
Cited by: 0 articles | PMID: 38922602 | PMCID: PMC11209175
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Sphingolipid and Trimethylamine-N-Oxide (TMAO) Levels in Women with Obesity after Combined Physical Training.
Brandao CFC, Krempf M, Giolo de Carvalho F, Aguesse A, Junqueira-Franco MVM, Batitucci G, de Freitas EC, Noronha NY, Rodrigues GDS, Junqueira GP, Borba DA, Billon-Crossouard S, Croyal M, Marchini JS
Metabolites, 14(8):398, 23 Jul 2024
Cited by: 0 articles | PMID: 39195494 | PMCID: PMC11355985
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A deep catalogue of protein-coding variation in 983,578 individuals.
Sun KY, Bai X, Chen S, Bao S, Zhang C, Kapoor M, Backman J, Joseph T, Maxwell E, Mitra G, Gorovits A, Mansfield A, Boutkov B, Gokhale S, Habegger L, Marcketta A, Locke AE, Ganel L, Hawes A, [...] Balasubramanian S
Nature, 631(8021):583-592, 20 May 2024
Cited by: 0 articles | PMID: 38768635 | PMCID: PMC11254753
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8-week Combined Exercise Protocol Promote Health and Cardiovascular Benefits in Obese Women by Epigenetic Modifications: a Prospective Study
Brandão CFC, Rodrigues GS, Noronha NY, Nicoletti CF, Junqueira-Franco MV, Alves CP, Diani LM, Carvalho FG, Freitas EC, Nonino CB, Marchini JS
Research Square, 25 Mar 2024
Cited by: 0 articles | PPR: PPR827345
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Data-driven, cross-disciplinary collaboration: lessons learned at the largest academic health center in Latin America during the COVID-19 pandemic.
Ritto AP, de Araujo AL, de Carvalho CRR, De Souza HP, Favaretto PMES, Saboya VRB, Garcia ML, Kulikowski LD, Kallás EG, Pereira AJR, Cobello Junior V, Silva KR, Abdalla ERF, Segurado AAC, Sabino EC, Ribeiro Junior U, Francisco RPV, Miethke-Morais A, Levin ASS, [...] Busatto Filho G
Front Public Health, 12:1369129, 27 Feb 2024
Cited by: 0 articles | PMID: 38476486 | PMCID: PMC10927964
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The Physician Surprise Question in the Emergency Department: prospective cohort study.
Ribeiro SCC, Arantes Lopes TA, Costa JVG, Rodrigues CG, Maia IWA, Soler LM, Marchini JFM, Neto RAB, Souza HP, Alencar JCG
BMJ Support Palliat Care, spcare-2024-004797, 05 Feb 2024
Cited by: 0 articles | PMID: 38316516
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Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Ziyatdinov A, Torres J, Alegre-Díaz J, Backman J, Mbatchou J, Turner M, Gaynor SM, Joseph T, Zou Y, Liu D, Wade R, Staples J, Panea R, Popov A, Bai X, Balasubramanian S, Habegger L, Lanche R, Lopez A, [...] Tapia-Conyer R
Nature, 626(8001):E18, 01 Feb 2024
Cited by: 0 articles | PMID: 38332034 | PMCID: PMC10901729
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A Genomics England haplotype reference panel and the imputation of the UK Biobank
Shi S, Rubinacci S, Hu S, Moutsianas L, Stuckey A, Need A, Caulfield M, Marchini J, Myers S
Research Square, 04 Dec 2023
Cited by: 0 articles | PPR: PPR768752
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A Genomics England haplotype reference panel and the imputation of the UK Biobank
Shi S, Rubinacci S, Hu S, Moutsianas L, Stuckey A, Need AC, The Genomics England Research Consortium, Caulfield M, Marchini J, Myers S
medRxiv, 08 Nov 2023
Cited by: 0 articles | PPR: PPR754926
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A large meta-analysis identifies genes associated with anterior uveitis.
Gelfman S, Moscati A, Huergo SM, Wang R, Rajagopal V, Parikshak N, Pounraja VK, Chen E, Leblanc M, Hazlewood R, Freudenberg J, Cooper B, Ligocki AJ, Miller CG, Van Zyl T, Weyne J, Romano C, Sagdullaev B, Melander O, [...] Coppola G
Nat Commun, 14(1):7300, 11 Nov 2023
Cited by: 2 articles | PMID: 37949852 | PMCID: PMC10638276
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Diabetes related phenotypes and their influence on outcomes of patients with corona virus disease 2019 (COVID-19).
Alves LI, Bosco AA, Rosa AA, Correia MRS, Matioli SR, da Silva MER, HCFMUSP COVID-19 Study Group
Diabetol Metab Syndr, 15(1):203, 16 Oct 2023
Cited by: 0 articles | PMID: 37845766 | PMCID: PMC10577940
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NOTCH3p.Arg1231Cys is Markedly Enriched in South Asians and Associated with Stroke
Rodriguez-Flores JL, Khalid S, Parikshak N, Rasheed A, Ye B, Kapoor M, Backman J, Sepehrband F, DiGioia SA, Gelfman S, De T, Banerjee N, Sharma D, Martinez H, Castaneda S, D’Ambrosio D, Zhang XA, Xun P, Tsai E, [...] Regeneron Genetics Center
medRxiv, 05 Oct 2023
Cited by: 0 articles | PPR: PPR736726
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Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Ziyatdinov A, Torres J, Alegre-Díaz J, Backman J, Mbatchou J, Turner M, Gaynor SM, Joseph T, Zou Y, Liu D, Wade R, Staples J, Panea R, Popov A, Bai X, Balasubramanian S, Habegger L, Lanche R, Lopez A, [...] Tapia-Conyer R
Nature, 622(7984):784-793, 11 Oct 2023
Cited by: 18 articles | PMID: 37821707 | PMCID: PMC10600010
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Yield of genetic association signals from genomes, exomes, and imputation in the UK biobank
Gaynor SM, Joseph T, Bai X, Krasheninina O, Boutkov B, Maxwell E, Balasubramanian S, Marcketta A, Backman J, Regeneron Genetics Center, Reid JG, Overton JD, Lotta LA, Marchini J, Salerno WJ, Baras A, Abecasis GR, Thornton TA
medRxiv, 13 Sep 2023
Cited by: 0 articles | PPR: PPR724815
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Author Correction: Sparse whole-genome sequencing identifies two loci for major depressive disorder.
CONVERGE consortium
Nature, 620(7976):E28, 01 Aug 2023
Cited by: 0 articles | PMID: 37567929
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Leveraging fine-scale population structure reveals conservation in genetic effect sizes between human populations across a range of human phenotypes
Hu S, Ferreira LAF, Shi S, Hellenthal G, Marchini J, Lawson DJ, Myers SR
bioRxiv, 09 Aug 2023
Cited by: 0 articles | PPR: PPR706893
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Polygenic risk prediction: why and when out-of-sample prediction R² can exceed SNP-based heritability.
Wang X, Walker A, Revez JA, Ni G, Adams MJ, McIntosh AM, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Visscher PM, Wray NR
Am J Hum Genet, 110(7):1207-1215, 27 Jun 2023
Cited by: 4 articles | PMID: 37379836 | PMCID: PMC10357496
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Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Rajagopal VM, Watanabe K, Mbatchou J, Ayer A, Quon P, Sharma D, Kessler MD, Praveen K, Gelfman S, Parikshak N, Otto JM, Bao S, Chim SM, Pavlopoulos E, Avbersek A, Kapoor M, Chen E, Jones MB, Leblanc M, [...] Coppola G
Nat Genet, 55(7):1138-1148, 12 Jun 2023
Cited by: 7 articles | PMID: 37308787 | PMCID: PMC10335934
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1-25 of 465 results

1 2 3 Next ...

Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Marchini J" with an ORCID

Search results

Joint testing of rare variant burden scores using non-negative least squares.

Benfotiamine Supplementation Increases Thiamine in Muscle of Endurance-Trained Mice and Affects the Energy Metabolism.

Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank.

Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone.

NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.

Genetic risk factors for COVID-19 and influenza are largely distinct.

A Genomics England haplotype reference panel and imputation of UK Biobank.

Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk.

Sphingolipid and Trimethylamine-N-Oxide (TMAO) Levels in Women with Obesity after Combined Physical Training.

A deep catalogue of protein-coding variation in 983,578 individuals.

8-week Combined Exercise Protocol Promote Health and Cardiovascular Benefits in Obese Women by Epigenetic Modifications: a Prospective Study

Data-driven, cross-disciplinary collaboration: lessons learned at the largest academic health center in Latin America during the COVID-19 pandemic.

The Physician Surprise Question in the Emergency Department: prospective cohort study.

Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

A Genomics England haplotype reference panel and the imputation of the UK Biobank

A Genomics England haplotype reference panel and the imputation of the UK Biobank

A large meta-analysis identifies genes associated with anterior uveitis.

Diabetes related phenotypes and their influence on outcomes of patients with corona virus disease 2019 (COVID-19).

NOTCH3p.Arg1231Cys is Markedly Enriched in South Asians and Associated with Stroke

Genotyping, sequencing and analysis of 140,000 adults from Mexico City.

Yield of genetic association signals from genomes, exomes, and imputation in the UK biobank

Author Correction: Sparse whole-genome sequencing identifies two loci for major depressive disorder.

Leveraging fine-scale population structure reveals conservation in genetic effect sizes between human populations across a range of human phenotypes

Polygenic risk prediction: why and when out-of-sample prediction R² can exceed SNP-based heritability.

Rare coding variants in CHRNB2 reduce the likelihood of smoking.

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Suggested authors matching "AUTH:Marchini J" with an ORCID